ICD-10 Code E70.320 | Tyrosinase negative oculocutaneous albinism Symptoms, Diagnosis, Billing

The main symptoms include a complete lack of pigmentation in the skin, hair, and eyes, increased sensitivity to sunlight, and visual impairments such as nystagmus and reduced visual acuity.

Diagnosis is typically made through clinical evaluation of symptoms, family history, and genetic testing to confirm mutations in the TYR gene.

There is no cure for this condition; management focuses on protective measures such as sun safety, regular skin checks, and vision correction as needed.

Yes, it is an autosomal recessive genetic disorder, meaning that both parents must carry the gene mutation for a child to be affected.